ID: ALA2426579

Max Phase: Preclinical

Molecular Formula: C14H11N3S2

Molecular Weight: 285.40

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  c1ccc(-c2nc(CSc3ncccn3)cs2)cc1

Standard InChI:  InChI=1S/C14H11N3S2/c1-2-5-11(6-3-1)13-17-12(9-18-13)10-19-14-15-7-4-8-16-14/h1-9H,10H2

Standard InChI Key:  UOFJARDSEYJTHA-UHFFFAOYSA-N

Associated Targets(non-human)

Deoxycytidine kinase 72 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 285.40Molecular Weight (Monoisotopic): 285.0394AlogP: 3.89#Rotatable Bonds: 4
Polar Surface Area: 38.67Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.80CX LogP: 3.53CX LogD: 3.53
Aromatic Rings: 3Heavy Atoms: 19QED Weighted: 0.54Np Likeness Score: -2.44

References

1. Murphy JM, Armijo AL, Nomme J, Lee CH, Smith QA, Li Z, Campbell DO, Liao HI, Nathanson DA, Austin WR, Lee JT, Darvish R, Wei L, Wang J, Su Y, Damoiseaux R, Sadeghi S, Phelps ME, Herschman HR, Czernin J, Alexandrova AN, Jung ME, Lavie A, Radu CG..  (2013)  Development of new deoxycytidine kinase inhibitors and noninvasive in vivo evaluation using positron emission tomography.,  56  (17): [PMID:23947754] [10.1021/jm400457y]

Source